Safety & Tolerability of TG1050: A Dose-finding Study

Clinical Trial Summary

Methodology:

This is a double-blind, randomized, placebo-controlled, multi-cohort Phase 1/1b study in patients that are currently being treated for chronic HBV infection. For all cohorts, patients must be receiving antiviral treatment with either tenofovir disoproxil fumarate (TDF) or entecavir (ENT) for at least two years, and have their HBV infection well-controlled

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NCT number	NCT02428400
Study type	Interventional
Source	Transgene
Contact
Status	Completed
Phase	Phase 1
Start date	October 2015
Completion date	November 2018

Safety and Tolerability of TG1050: A Dose-finding Study

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms